Impact of polypharmacy on all-cause mortality and hospitalization in incident hemodialysis patients: a cohort study.


Journal

Clinical and experimental nephrology
ISSN: 1437-7799
Titre abrégé: Clin Exp Nephrol
Pays: Japan
ID NLM: 9709923

Informations de publication

Date de publication:
Nov 2021
Historique:
received: 21 02 2021
accepted: 08 06 2021
pubmed: 16 6 2021
medline: 27 1 2022
entrez: 15 6 2021
Statut: ppublish

Résumé

Polypharmacy (PP) is common in end-stage chronic renal disease patients largely due to the presence of multiple comorbid conditions. Although PP is potentially harmful, its relationship with mortality and morbidity in hemodialysis patients currently remains unclear. Study design: cohort study. participants: one hundred and fifty-two initial hemodialysis patients (male, 88 patients; mean age, 70.3 years) were enrolled between February 2015 and March 2018 at Nobeoka Prefectural Hospital and Chiyoda Hospital. patients were divided into 2 groups according to PP (6 or more drug prescriptions or less) during admission and discharge for the initiation of hemodialysis. all-cause mortality and hospitalization during the mean 2.8-year follow-up. hazard ratios (HRs) were estimated using Cox's model for the relationships between PP and clinical outcomes and adjusted for potential confounders. The group with 5 or less drug prescriptions was set as a reference. The number of prescribed drugs per patient averaged 7.4 at admission and 7.0 at discharge for initial hemodialysis. One hundred (65.8%) and 94 patients (61.8%) had PP at admission and discharge, respectively. During the follow-up, 20 patients died and 71 were hospitalized. PP at admission did not correlate with outcomes, whereas that at discharge correlated with all-cause hospitalization. PP at discharge may be associated with clinical outcomes. However, it remains unclear whether PP is the direct cause of outcomes or is simply a marker for an increased risk of outcomes.

Sections du résumé

BACKGROUND BACKGROUND
Polypharmacy (PP) is common in end-stage chronic renal disease patients largely due to the presence of multiple comorbid conditions. Although PP is potentially harmful, its relationship with mortality and morbidity in hemodialysis patients currently remains unclear.
METHODS METHODS
Study design: cohort study.
SETTING METHODS
participants: one hundred and fifty-two initial hemodialysis patients (male, 88 patients; mean age, 70.3 years) were enrolled between February 2015 and March 2018 at Nobeoka Prefectural Hospital and Chiyoda Hospital.
PREDICTOR METHODS
patients were divided into 2 groups according to PP (6 or more drug prescriptions or less) during admission and discharge for the initiation of hemodialysis.
OUTCOMES RESULTS
all-cause mortality and hospitalization during the mean 2.8-year follow-up.
MEASUREMENTS METHODS
hazard ratios (HRs) were estimated using Cox's model for the relationships between PP and clinical outcomes and adjusted for potential confounders. The group with 5 or less drug prescriptions was set as a reference.
RESULTS RESULTS
The number of prescribed drugs per patient averaged 7.4 at admission and 7.0 at discharge for initial hemodialysis. One hundred (65.8%) and 94 patients (61.8%) had PP at admission and discharge, respectively. During the follow-up, 20 patients died and 71 were hospitalized. PP at admission did not correlate with outcomes, whereas that at discharge correlated with all-cause hospitalization.
CONCLUSIONS CONCLUSIONS
PP at discharge may be associated with clinical outcomes. However, it remains unclear whether PP is the direct cause of outcomes or is simply a marker for an increased risk of outcomes.

Identifiants

pubmed: 34129133
doi: 10.1007/s10157-021-02094-9
pii: 10.1007/s10157-021-02094-9
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1215-1223

Informations de copyright

© 2021. Japanese Society of Nephrology.

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Auteurs

Tatsunori Toida (T)

Department of Hemovascular Medicine and Artificial Organs, Faculty of Medicine, University of Miyazaki, 5200 Kihara Kiyotake, Miyazaki city, Miyazaki, 889-1692, Japan. t.toida@med.miyazaki-u.ac.jp.
Department of Internal Medicine, Miyazaki Prefectural Nobeoka Hospital, Nobeoka City, Miyazaki, Japan. t.toida@med.miyazaki-u.ac.jp.

Reiko Toida (R)

Chiyoda Hospital, Hyuga city, Miyazaki, Japan.

Risa Takahashi (R)

Department of Internal Medicine, Miyazaki Prefectural Nobeoka Hospital, Nobeoka City, Miyazaki, Japan.

Shigehiro Uezono (S)

Chiyoda Hospital, Hyuga city, Miyazaki, Japan.

Hiroyuki Komatsu (H)

Center for Medical Education and Career Development, Faculty of Medicine, University of Miyazaki, Miyazaki city, Miyazaki, Japan.

Yuji Sato (Y)

Division of Nephrology, Department of Internal Medicine, National Health Insurance Takachiho Town Hospital, Takachiho, Miyazaki, Japan.

Shouichi Fujimoto (S)

Department of Hemovascular Medicine and Artificial Organs, Faculty of Medicine, University of Miyazaki, 5200 Kihara Kiyotake, Miyazaki city, Miyazaki, 889-1692, Japan.

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